Exploring the impact of Anaplasma phagocytophilum on colonization resistance of Ixodes scapularis microbiota using network node manipulation

• Published in: Current research in parasitology & vector-borne diseases Vol. 5; p. 100177
• Main Authors: Abuin-Denis, Lianet, Piloto-Sardiñas, Elianne, Maître, Apolline, Wu-Chuang, Alejandra, Mateos-Hernández, Lourdes, Obregon, Dasiel, Corona-González, Belkis, Fogaça, Andréa Cristina, Palinauskas, Vaidas, Aželytė, Justė, Rodríguez-Mallon, Alina, Cabezas-Cruz, Alejandro
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-01-2024; Elsevier
• Subjects: Colonization resistance; Community assembly; from the special issue on Recent trends and future prospects in genetics and genomics of parasites and vectors; Edited by Dr Frank Katzer and Professor Aneta Kostadinova; Life Sciences; Microbiology and Parasitology; Parasitology; Tick-borne pathogens; Ticks; Colonization resistance; Community assembly; Tick-borne pathogens; Ticks
• ISSN: 2667-114X; 2667-114X
• DOI: 10.1016/j.crpvbd.2024.100177

Upon ingestion from an infected host, tick-borne pathogens (TBPs) have to overcome colonization resistance, a defense mechanism by which tick microbiota prevent microbial invasions. Previous studies have shown that the pathogen Anaplasma phagocytophilum alters the microbiota composition of the nymphs of Ixodes scapularis, but its impact on tick colonization resistance remains unclear. We analyzed tick microbiome genetic data using published Illumina 16S rRNA sequences, assessing microbial diversity within ticks (alpha diversity) through species richness, evenness, and phylogenetic diversity. We compared microbial communities in ticks with and without infection with A. phagocytophilum (beta diversity) using the Bray-Curtis index. We also built co-occurrence networks and used node manipulation to study the impact of A. phagocytophilum on microbial assembly and network robustness, crucial for colonization resistance. We examined network robustness by altering its connectivity, observing changes in the largest connected component (LCC) and the average path length (APL). Our findings revealed that infection with A. phagocytophilum does not significantly alter the overall microbial diversity in ticks. Despite a decrease in the number of nodes and connections within the microbial networks of infected ticks, certain core microbes remained consistently interconnected, suggesting a functional role. The network of infected ticks showed a heightened vulnerability to node removal, with smaller LCC and longer APL, indicating reduced resilience compared to the network of uninfected ticks. Interestingly, adding nodes to the network of infected ticks led to an increase in LCC and a decrease in APL, suggesting a recovery in network robustness, a trend not observed in networks of uninfected ticks. This improvement in network robustness upon node addition hints that infection with A. phagocytophilum might lower ticksʼ resistance to colonization, potentially facilitating further microbial invasions. We conclude that the compromised colonization resistance observed in tick microbiota following infection with A. phagocytophilum may facilitate co-infection in natural tick populations.
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•Anaplasma phagocytophilum alters community assembly more than diversity in ticks.•Disruption of community assembly was associated with reduced network robustness.•Low network robustness links to weaker colonization resistance.•Adding nodes improved network robustness in A. phagocytophilum-infected ticks.•A. phagocytophilum reduces colonization resistance which may promote co-infections.